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Journal Abstract Search

192 related items for PubMed ID: 35457051

  • 21. Sequence variation in SORL1 and dementia risk in Swedes.
    Reynolds CA, Hong MG, Eriksson UK, Blennow K, Johansson B, Malmberg B, Berg S, Gatz M, Pedersen NL, Bennet AM, Prince JA.
    Neurogenetics; 2010 Feb; 11(1):139-42. PubMed ID: 19653016
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  • 25. Association of SORL1 gene variants with Alzheimer's disease.
    Kölsch H, Jessen F, Wiltfang J, Lewczuk P, Dichgans M, Teipel SJ, Kornhuber J, Frölich L, Heuser I, Peters O, Wiese B, Kaduszkiewicz H, van den Bussche H, Hüll M, Kurz A, Rüther E, Henn FA, Maier W.
    Brain Res; 2009 Apr 06; 1264():1-6. PubMed ID: 19368828
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  • 29. Expression of an alternatively spliced variant of SORL1 in neuronal dendrites is decreased in patients with Alzheimer's disease.
    Monti G, Kjolby M, Jensen AMG, Allen M, Reiche J, Møller PL, Comaposada-Baró R, Zolkowski BE, Vieira C, Jørgensen MM, Holm IE, Valdmanis PN, Wellner N, Vægter CB, Lincoln SJ, Nykjær A, Ertekin-Taner N, Young JE, Nyegaard M, Andersen OM.
    Acta Neuropathol Commun; 2021 Mar 16; 9(1):43. PubMed ID: 33726851
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  • 30. A genetically modified minipig model for Alzheimer's disease with SORL1 haploinsufficiency.
    Andersen OM, Bøgh N, Landau AM, Pløen GG, Jensen AMG, Monti G, Ulhøi BP, Nyengaard JR, Jacobsen KR, Jørgensen MM, Holm IE, Kristensen ML, Alstrup AKO, Hansen ESS, Teunissen CE, Breidenbach L, Droescher M, Liu Y, Pedersen HS, Callesen H, Luo Y, Bolund L, Brooks DJ, Laustsen C, Small SA, Mikkelsen LF, Sørensen CB.
    Cell Rep Med; 2022 Sep 20; 3(9):100740. PubMed ID: 36099918
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  • 32. Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls.
    Bellenguez C, Charbonnier C, Grenier-Boley B, Quenez O, Le Guennec K, Nicolas G, Chauhan G, Wallon D, Rousseau S, Richard AC, Boland A, Bourque G, Munter HM, Olaso R, Meyer V, Rollin-Sillaire A, Pasquier F, Letenneur L, Redon R, Dartigues JF, Tzourio C, Frebourg T, Lathrop M, Deleuze JF, Hannequin D, Genin E, Amouyel P, Debette S, Lambert JC, Campion D, CNR MAJ collaborators.
    Neurobiol Aging; 2017 Nov 20; 59():220.e1-220.e9. PubMed ID: 28789839
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  • 33. Genetic Study of Alzheimer's Disease in Saudi Population.
    El Bitar F, Qadi N, Al Rajeh S, Majrashi A, Abdulaziz S, Majrashi N, Al Inizi M, Taher A, Al Tassan N.
    J Alzheimers Dis; 2019 Nov 20; 67(1):231-242. PubMed ID: 30636737
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  • 34. Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease.
    T Cuenco K, Lunetta KL, Baldwin CT, McKee AC, Guo J, Cupples LA, Green RC, St George-Hyslop PH, Chui H, DeCarli C, Farrer LA, MIRAGE Study Group.
    Arch Neurol; 2008 Dec 20; 65(12):1640-8. PubMed ID: 19064752
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  • 37. The association between genetic variants in SORL1 and Alzheimer disease in an urban, multiethnic, community-based cohort.
    Lee JH, Cheng R, Schupf N, Manly J, Lantigua R, Stern Y, Rogaeva E, Wakutani Y, Farrer L, St George-Hyslop P, Mayeux R.
    Arch Neurol; 2007 Apr 20; 64(4):501-6. PubMed ID: 17420311
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  • 38. Endolysosome and autophagy dysfunction in Alzheimer disease.
    Hung C, Livesey FJ.
    Autophagy; 2021 Nov 20; 17(11):3882-3883. PubMed ID: 34429033
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  • 39. SorLA Protective Function Is Restored by Improving SorLA Protein Maturation in a Subset of Alzheimer's Disease-Associated SORL1 Missense Variants.
    Miguel L, Gervais J, Nicolas G, Lecourtois M.
    J Alzheimers Dis; 2023 Nov 20; 94(4):1343-1349. PubMed ID: 37424467
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  • 40. Influence of SORL1 gene variants: association with CSF amyloid-beta products in probable Alzheimer's disease.
    Kölsch H, Jessen F, Wiltfang J, Lewczuk P, Dichgans M, Kornhuber J, Frölich L, Heuser I, Peters O, Schulz JB, Schwab SG, Maier W.
    Neurosci Lett; 2008 Jul 25; 440(1):68-71. PubMed ID: 18541377
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